{
  "url": "https://dantelabs.com/el/genes/atp11a",
  "gene": {
    "slug": "atp11a",
    "symbol": "ATP11A",
    "name": "ATPase phospholipid transporting 11A",
    "hgnc": "HGNC:13552",
    "summary": null,
    "location": "13q34",
    "locusType": "gene with protein product",
    "aliases": [
      "ATPIH",
      "ATPIS",
      "KIAA1021"
    ],
    "previousSymbols": [],
    "ensemblId": "ENSG00000068650",
    "entrezId": 23250,
    "omim": [
      "605868"
    ],
    "uniprot": [
      "P98196"
    ],
    "model": {
      "build": "GRCh38",
      "release": "v1.5",
      "chrom": "13",
      "start": 112690038,
      "end": 112887168,
      "strand": "+",
      "ensemblTranscript": "ENST00000375645.8",
      "refseqTranscript": "NM_015205.3",
      "ensemblProtein": "ENSP00000364796.3",
      "refseqProtein": "NP_056020.2",
      "exons": [
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      ],
      "cds": {
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    },
    "grch37": {
      "build": "GRCh37",
      "release": "87",
      "chrom": "13",
      "start": 113344643,
      "end": 113541482,
      "strand": "+"
    },
    "neighbourhood": {
      "release": "116",
      "start": 112288603,
      "end": 113288602,
      "genes": [
        {
          "symbol": "SPACA7",
          "ensemblId": "ENSG00000153498",
          "biotype": "protein_coding",
          "start": 112376309,
          "end": 112434695,
          "strand": "+",
          "slug": "spaca7"
        },
        {
          "symbol": "TUBGCP3",
          "ensemblId": "ENSG00000126216",
          "biotype": "protein_coding",
          "start": 112485005,
          "end": 112588205,
          "strand": "-",
          "slug": "tubgcp3"
        },
        {
          "symbol": "MCF2L",
          "ensemblId": "ENSG00000126217",
          "biotype": "protein_coding",
          "start": 112894330,
          "end": 113100412,
          "strand": "+",
          "slug": "mcf2l"
        },
        {
          "symbol": "F7",
          "ensemblId": "ENSG00000057593",
          "biotype": "protein_coding",
          "start": 113105762,
          "end": 113120685,
          "strand": "+",
          "slug": "f7"
        },
        {
          "symbol": "F10",
          "ensemblId": "ENSG00000126218",
          "biotype": "protein_coding",
          "start": 113122771,
          "end": 113149531,
          "strand": "+",
          "slug": "f10"
        },
        {
          "symbol": "PROZ",
          "ensemblId": "ENSG00000126231",
          "biotype": "protein_coding",
          "start": 113158388,
          "end": 113173625,
          "strand": "+",
          "slug": "proz"
        },
        {
          "symbol": "PCID2",
          "ensemblId": "ENSG00000126226",
          "biotype": "protein_coding",
          "start": 113177117,
          "end": 113209458,
          "strand": "-",
          "slug": "pcid2"
        },
        {
          "symbol": "CUL4A",
          "ensemblId": "ENSG00000139842",
          "biotype": "protein_coding",
          "start": 113208193,
          "end": 113267108,
          "strand": "+",
          "slug": "cul4a"
        }
      ],
      "truncated": false
    },
    "reports": [
      {
        "slug": "hearing-loss-and-deafness",
        "name": "Απώλεια ακοής και κώφωση",
        "diseases": [
          {
            "mondoId": "MONDO:0021944",
            "name": "Νευροπάθεια ακουστικού νεύρου",
            "genes": 3,
            "inheritance": null,
            "description": "Απώλεια ακοής κατά την οποία το έσω ους ανιχνεύει τον ήχο, αλλά το σήμα δεν μεταδίδεται κανονικά στο ακουστικό νεύρο, συμπεριλαμβανομένων των κληρονομικών μορφών που προκαλούνται από το OTOF και άλλα γονίδια.",
            "management": "Ο προσδιορισμός της αιτίας μπορεί να επηρεάσει την επιλογή μεταξύ ακουστικών βαρηκοΐας και εμφυτευμάτων κοχλία, ενώ οι μορφές που σχετίζονται με το OTOF αποτελούν αντικείμενο κλινικών δοκιμών γονιδιακής θεραπείας.",
            "evidence": {
              "gencc": [
                "Labcorp Genetics (formerly Invitae)"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant"
              ]
            },
            "sameAsReport": false,
            "broad": false
          },
          {
            "mondoId": "MONDO:0019587",
            "name": "Αυτοσωμικά επικρατής μη συνδρομική απώλεια ακοής",
            "genes": 39,
            "inheritance": "autosomal-dominant",
            "description": "Αυτοσωμικά επικρατής μορφή μη συνδρομικής κώφωσης.",
            "management": null,
            "evidence": {
              "gencc": [
                "PanelApp Australia"
              ],
              "clingen": "Moderate",
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant"
              ]
            },
            "sameAsReport": false,
            "broad": false
          },
          {
            "mondoId": "MONDO:0019497",
            "name": "Μη συνδρομική γενετική απώλεια ακοής",
            "genes": 97,
            "inheritance": null,
            "description": "Κληρονομική απώλεια ακοής χωρίς άλλα ιατρικά συμπτώματα, συμπεριλαμβανομένων των συχνών υπολειπόμενων μορφών που προκαλούνται από τα GJB2, OTOF, SLC26A4, STRC και πολλά άλλα γονίδια, καθώς και των επικρατουσών, των φυλοσύνδετων και των μιτοχονδριακών μορφών.",
            "management": "Η γνώση της γενετικής αιτίας μπορεί να καθοδηγήσει την υποστήριξη ακοής και τις αποφάσεις για εμφύτευμα κοχλία, την επιλεξιμότητα για κλινικές δοκιμές γονιδιακής θεραπείας (για παράδειγμα για το OTOF) και τη γενετική συμβουλευτική της οικογένειας.",
            "evidence": {
              "gencc": [
                "PanelApp Australia"
              ],
              "clingen": "Moderate",
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant"
              ]
            },
            "sameAsReport": false,
            "broad": true
          }
        ],
        "url": "https://dantelabs.com/el/conditions/hearing-loss-and-deafness"
      },
      {
        "slug": "pelizaeus-merzbacher-and-hypomyelinating-leukodystrophies",
        "name": "Νόσος Pelizaeus-Merzbacher και υπομυελινωτικές λευκοδystροφίες",
        "diseases": [
          {
            "mondoId": "MONDO:0859242",
            "name": "Υπομυελινωτική λευκοδystροφία 24 (ATP11A)",
            "genes": 1,
            "inheritance": "autosomal-dominant",
            "description": "Σπάνια κληρονομική μορφή υπομυελινωτικής λευκοδystροφίας, κατά την οποία η μυελίνη του εγκεφάλου δεν σχηματίζεται φυσιολογικά, προκαλώντας καθυστερημένη ανάπτυξη και κινητικά προβλήματα.",
            "management": null,
            "evidence": {
              "gencc": [
                "PanelApp Australia"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant"
              ]
            },
            "sameAsReport": false,
            "broad": false
          }
        ],
        "url": "https://dantelabs.com/el/conditions/pelizaeus-merzbacher-and-hypomyelinating-leukodystrophies"
      },
      {
        "slug": "leukodystrophy",
        "name": "Άλλες κληρονομικές λευκοδystrοφίες",
        "diseases": [
          {
            "mondoId": "MONDO:0019046",
            "name": "Λευκοδυστροφία (άλλοι και μη προσδιορισμένοι τύποι)",
            "genes": 80,
            "inheritance": null,
            "description": "Κληρονομικές παθήσεις που βλάπτουν ή εμποδίζουν τον φυσιολογικό σχηματισμό της μυελίνης, της λευκής ουσίας του εγκεφάλου και του νωτιαίου μυελού. Οι διαφορετικοί τύποι ακολουθούν αυτοσωμική υπολειπόμενη, αυτοσωμική επικρατή ή X-συνδεδεμένη κληρονομικότητα, ανάλογα με το εμπλεκόμενο γονίδιο.",
            "management": "Η γνώση της συγκεκριμένης γενετικής αιτίας μπορεί να τερματίσει τη διαγνωστική αναζήτηση, να καθοδηγήσει τη υποστηρικτική φροντίδα και την παρακολούθηση, να δείξει αν υπάρχει συγκεκριμένη θεραπεία και να επιτρέψει τον έλεγχο των συγγενών.",
            "evidence": {
              "gencc": [
                "PanelApp Australia"
              ],
              "acmgSf": false,
              "inheritance": [
                "autosomal-dominant"
              ]
            },
            "sameAsReport": false,
            "broad": true
          }
        ],
        "url": "https://dantelabs.com/el/conditions/leukodystrophy"
      }
    ],
    "pharmacogenomics": [],
    "traits": [],
    "phenotypes": [
      {
        "slug": "abnormal-speech-discrimination",
        "name": "Abnormal speech discrimination",
        "systems": [
          "abnormality-of-the-ear"
        ],
        "url": "https://dantelabs.com/traits/abnormal-speech-discrimination"
      },
      {
        "slug": "abnormal-pulmonary-interstitial-morphology",
        "name": "Abnormality in area between air sacs in lung",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "very-frequent",
        "url": "https://dantelabs.com/traits/abnormal-pulmonary-interstitial-morphology"
      },
      {
        "slug": "microcephaly",
        "name": "Abnormally small head",
        "systems": [
          "abnormality-of-head-or-neck",
          "abnormality-of-the-musculoskeletal-system",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/microcephaly"
      },
      {
        "slug": "areflexia",
        "name": "Absent reflexes",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/areflexia"
      },
      {
        "slug": "gastroesophageal-reflux",
        "name": "Acid reflux",
        "systems": [
          "abnormality-of-the-digestive-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/gastroesophageal-reflux"
      },
      {
        "slug": "cataract",
        "name": "Clouding of the lens of the eye",
        "systems": [
          "abnormality-of-the-eye"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/cataract"
      },
      {
        "slug": "clubbing-of-fingers",
        "name": "Clubbing of fingers",
        "systems": [
          "abnormality-of-limbs",
          "abnormality-of-the-musculoskeletal-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/clubbing-of-fingers"
      },
      {
        "slug": "cough",
        "name": "Cough",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/cough"
      },
      {
        "slug": "crackles",
        "name": "Crackles",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/crackles"
      },
      {
        "slug": "exercise-intolerance",
        "name": "Decreased ability to exercise",
        "systems": [
          "constitutional-symptom"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/exercise-intolerance"
      },
      {
        "slug": "decreased-dlco",
        "name": "Decreased DLCO",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/decreased-dlco"
      },
      {
        "slug": "decreased-motor-nerve-conduction-velocity",
        "name": "Decreased motor nerve conduction velocity",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/decreased-motor-nerve-conduction-velocity"
      },
      {
        "slug": "cerebral-atrophy",
        "name": "Degeneration of cerebrum",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/cerebral-atrophy"
      },
      {
        "slug": "seizure",
        "name": "Epilepsy",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/seizure"
      },
      {
        "slug": "exertional-dyspnea",
        "name": "Exertional breathlessness",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/exertional-dyspnea"
      },
      {
        "slug": "fatigue",
        "name": "Fatigue",
        "systems": [
          "constitutional-symptom"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/fatigue"
      },
      {
        "slug": "flexion-contracture",
        "name": "Flexed joint that cannot be straightened",
        "systems": [
          "abnormality-of-the-musculoskeletal-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/flexion-contracture"
      },
      {
        "slug": "global-developmental-delay",
        "name": "Global developmental delay",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/global-developmental-delay"
      },
      {
        "slug": "ground-glass-opacification",
        "name": "Ground-glass opacification",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/ground-glass-opacification"
      },
      {
        "slug": "honeycomb-lung",
        "name": "Honeycomb lung",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/honeycomb-lung"
      },
      {
        "slug": "leukodystrophy",
        "name": "Leukodystrophy",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/leukodystrophy"
      },
      {
        "slug": "developmental-regression",
        "name": "Loss of developmental milestones",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/developmental-regression"
      },
      {
        "slug": "decreased-total-b-cell-count",
        "name": "Low B cell count",
        "systems": [
          "abnormality-of-blood-and-blood-forming-tissues",
          "abnormality-of-the-immune-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/decreased-total-b-cell-count"
      },
      {
        "slug": "orthodeoxia",
        "name": "Orthodeoxia",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/orthodeoxia"
      },
      {
        "slug": "peripheral-axonal-neuropathy",
        "name": "Peripheral axonal neuropathy",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/peripheral-axonal-neuropathy"
      },
      {
        "slug": "bronchiectasis",
        "name": "Permanent enlargement of the airways of the lungs",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/bronchiectasis"
      },
      {
        "slug": "acrocyanosis",
        "name": "Persistent blue color of hands or feet",
        "systems": [
          "abnormality-of-the-integument"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/acrocyanosis"
      },
      {
        "slug": "pulmonary-fibrosis",
        "name": "Pulmonary scarring",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/pulmonary-fibrosis"
      },
      {
        "slug": "pulmonic-regurgitation",
        "name": "Pulmonic regurgitation",
        "systems": [
          "abnormality-of-the-cardiovascular-system"
        ],
        "frequency": "occasional",
        "url": "https://dantelabs.com/traits/pulmonic-regurgitation"
      },
      {
        "slug": "reduced-forced-vital-capacity",
        "name": "Reduced forced vital capacity",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/reduced-forced-vital-capacity"
      },
      {
        "slug": "reticular-pattern-on-pulmonary-hrct",
        "name": "Reticular pattern on pulmonary HRCT",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/reticular-pattern-on-pulmonary-hrct"
      },
      {
        "slug": "sensorineural-hearing-impairment",
        "name": "Sensorineural hearing impairment",
        "systems": [
          "abnormality-of-the-ear"
        ],
        "url": "https://dantelabs.com/traits/sensorineural-hearing-impairment"
      },
      {
        "slug": "severe-short-stature",
        "name": "Severe short stature",
        "systems": [
          "growth-abnormality"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/severe-short-stature"
      },
      {
        "slug": "subpleural-honeycombing",
        "name": "Subpleural honeycombing",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/subpleural-honeycombing"
      },
      {
        "slug": "thin-corpus-callosum",
        "name": "Thin corpus callosum",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/thin-corpus-callosum"
      },
      {
        "slug": "tongue-fasciculations",
        "name": "Tongue twitching",
        "systems": [
          "abnormality-of-head-or-neck",
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/tongue-fasciculations"
      },
      {
        "slug": "hypothyroidism",
        "name": "Underactive thyroid",
        "systems": [
          "abnormality-of-the-endocrine-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/hypothyroidism"
      },
      {
        "slug": "usual-interstitial-pneumonia",
        "name": "Usual interstitial pneumonia",
        "systems": [
          "abnormality-of-the-respiratory-system"
        ],
        "frequency": "frequent",
        "url": "https://dantelabs.com/traits/usual-interstitial-pneumonia"
      },
      {
        "slug": "ventriculomegaly",
        "name": "Ventriculomegaly",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/ventriculomegaly"
      },
      {
        "slug": "widened-subarachnoid-space",
        "name": "Widened subarachnoid space",
        "systems": [
          "abnormality-of-the-nervous-system"
        ],
        "frequency": "obligate",
        "url": "https://dantelabs.com/traits/widened-subarachnoid-space"
      }
    ],
    "related": [
      {
        "slug": "actg1",
        "symbol": "ACTG1",
        "name": "actin gamma 1",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/actg1"
      },
      {
        "slug": "aifm1",
        "symbol": "AIFM1",
        "name": "apoptosis inducing factor mitochondria associated 1",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/aifm1"
      },
      {
        "slug": "atp2b2",
        "symbol": "ATP2B2",
        "name": "ATPase plasma membrane Ca2+ transporting 2",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/atp2b2"
      },
      {
        "slug": "cd164",
        "symbol": "CD164",
        "name": "CD164 molecule",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/cd164"
      },
      {
        "slug": "ceacam16",
        "symbol": "CEACAM16",
        "name": "CEA cell adhesion molecule 16, tectorial membrane component",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/ceacam16"
      },
      {
        "slug": "coch",
        "symbol": "COCH",
        "name": "cochlin",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/coch"
      },
      {
        "slug": "col11a1",
        "symbol": "COL11A1",
        "name": "collagen type XI alpha 1 chain",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/col11a1"
      },
      {
        "slug": "col11a2",
        "symbol": "COL11A2",
        "name": "collagen type XI alpha 2 chain",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/col11a2"
      },
      {
        "slug": "diaph1",
        "symbol": "DIAPH1",
        "name": "diaphanous related formin 1",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/diaph1"
      },
      {
        "slug": "eya4",
        "symbol": "EYA4",
        "name": "EYA transcriptional coactivator and phosphatase 4",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/eya4"
      },
      {
        "slug": "gjb2",
        "symbol": "GJB2",
        "name": "gap junction protein beta 2",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/gjb2"
      },
      {
        "slug": "gjb6",
        "symbol": "GJB6",
        "name": "gap junction protein beta 6",
        "shared": 2,
        "url": "https://dantelabs.com/el/genes/gjb6"
      }
    ],
    "sources": {
      "bundleId": "2026.10.17-8666dff2",
      "panel": "2026-10-17",
      "acmgSf": "SF v3.2"
    },
    "locusKind": "proteinCoding"
  },
  "variants": {
    "total": 0,
    "url": null,
    "items": []
  }
}